ISO 18113-3:2009

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use

Publication date: 9 dhj 2009

95.99 Withdrawal of Standard 6 tet 2022

General information

Current stage: 95.99 Effective date: 6 tet 2022

Originator: ISO

Owner: ISO/TC 212

Type: International Standard

ICS: 11.100.10

Gjuha: anglisht frëngjisht

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Statusi: Shfuqizuar

PDF - 7 123 Lekë

Paper - 7 123 Lekë

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Scope

ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.
ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
ISO 18113-3:2009 can also be applied to accessories, where appropriate.

ISO 18113-3:2009

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use

95.99 Withdrawal of Standard 6 tet 2022

General information

Buying

Scope

Life cycle

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